| Tag | Content |
|---|
EnhancerAtlas ID | HS043-21840 |
Organism | Homo sapiens |
Tissue/cell | Fetal_heart |
Coordinate | chr2:24657310-24659480 |
SNPs | | Number: 1 | ID | Chromosome | Position | Genome Version |
|
TF binding sites/motifs | | TF | JASPAR ID | Coordinate | Motif Sequence | Strand | -Log10(p-value) |
| MIXL1 | MA0662.1 | chr2:24658558-24658568 | TCTAATTAAC | + | 6.02 | | Myog | MA0500.1 | chr2:24659041-24659052 | GACAGCTGCAG | + | 6.62 | | Tcf12 | MA0521.1 | chr2:24659041-24659052 | GACAGCTGCAG | + | 6.14 |
|
| | Diseases: AD,Huntington,Obesity,Parkinson,Prostate cancer,Schizophrenia and Sleep disorder | | Number of disease enhancers: 1 | Chromosome | Start | End |
|
| | Number: 1 | ID | Chromosome | Start | End |
| GH02I024433 | chr2 | 24656789 | 24659939 |
|
Enhancer Sequence | TGTTAGAAGA AAGGGTCTGA AAGGTTCAAT TAGAGACTCA AGATCTGTGG GGTTCCCAGC 60
TGTCCCTGGA GCAAGGTACC CTTGACAGCC AGTCTATGGT CTATGAGAGC GTGAAGTTGA 120
TTCCTTTTCC TCCAGCTTCC TTTGGGTCTT TCCCCAACCT GGCCTTGGGC AAGGCTGACT 180
CTGGGTTGCT TTTCTGTTGC TGTTACTCCC TGGAATTGGA CCCATAGTTT GAGCCTCCTC 240
TGGAAAAGGG ATCACAAGTC TCTCCTTACA CTGCTGGCTC CAGGTCACCT CCTGTAGGCC 300
AGGCCTGGGG GGTGGAGTTG GCCAGAGCAC TAAACTATCT GGGGTATGCT CTGGGCCTCT 360
TGGCTGAGAA GGCCAAAACA CTCACCATCA GCTCTGCTAT TTTCTCTCTC CCCAGGACCT 420
GGGGAGAAAG GAGGAAGAGC CACTTCTCTT ATCACTGTCT TTGGCTGGTC TCATCCATTC 480
CTCTTCCATC CTTCATGCCT CCTCCTCTCT CTGTGTCATG GTCCCCATTT TTTTCTCCCT 540
GATCACTGTC CCTCTGACAG TGTTTCTGAC TTCCAGAGTT CATTTTGAGG CCTCTCTTCC 600
TCATCTTCTC TCCTTTCCCA CCTAGACCGA GCTCTTGTCA GCCCACCTTT CTGTTTCTGG 660
CTGTTTCCAC TGTTGTTCCC TGTCCGCAGA GCAAACGGGG CAGGGAGGCG ATGCCACCCT 720
TGTGGGCCCG GCAGGGAGCT GGGTGATTTT TAAGCGTTTT TCTCATTTTA AGGGCTAGGT 780
GATAGAATGG TTGCCTGAGG CCCCACCTCA GAAGCTGGCC TAGGGTCCCG ACAGGAGTTG 840
TCTCACACTC CGTCCCACGG AACTGGGGGT GAGGTGGTGG CAGTGCTGGC ATCAGACCAT 900
AACATAAAGG GAGTAGCTGA AGCCCTCCGA AGTAGGCCAC GCCTGCGCCA TTGCACAGTT 960
CGGAGCTCTC CCATCAGCCC TTCCGAGTGC ACTGCCTCAA GTCGCACATC CAAAGTGAAA 1020
TGTGGGTGTT TTAATCACTG AAGAGAATCC TTAATGCTGC TCCTTCAGCA CATAGCTGTC 1080
TCTCCTGTGC CAGGAACCGC AGGGAGCCTA TTGCTTTCCA TCCTGAACTG GATCCAGAAG 1140
CGTTAGGTGA GGCTCAATAC AATTTTCAGT TGTTATCATG GGAGGCCCTT AGAGACGCTT 1200
CTCAGTTCTA GCAATTAGCC ACACAGGGGT CAACCAAGTG TTCTCAGCTC TAATTAACAG 1260
CTGTGTTGAA TCTGGGACAC ATAGAATTCC TTTGGGGACG CACTCTTCAA ACAGAAACAA 1320
AGCCAGAATA GCAAGCTCTT TCCTCCTTAT CAGAGGCTAT GAAGTATGAA AATGACTGCT 1380
GAGGGGATTC TTAATGAAAA TACCGGGAAG CTGAGTGGCC TCCGGGCTGC ATGTATGAAT 1440
TTAAAGGCAA AAAGACAATC TCAGCTTGAC TATGAAGTTA TCTGCTGGGG CTCAGGAGGC 1500
TCTGGGGAGC GCTGGGGGAA TTAGGTGCCT CTTAGCTCCA CTCCCAGAGC CCGGTACACC 1560
CAGCAGGCTA CATGATAATC ATCACCACAC AAATCAAAGG CTTGATCTCT GGCTTCAAAA 1620
GGAAAAGGAA CAGGAACAGG ATACTCTCTG TTGGGACTCC TGCTCTGAGC GGGAACTATG 1680
CTGATGCCTG TTCAAGTTGT TCCCTGGGTA TTTTGGCTTC TTGCCCTGCC TGACAGCTGC 1740
AGGAGTTCTG TAAGAAATCT GAGGGAGAAT TTCCTTTGCA ACCATGACTG AGAACCCAGG 1800
ATCAAGAGCT TTGCAGACAG AAAAGACATT ACCCTTCGAA TATCCCAAGC CATCTATTAG 1860
GGTCAGCAAG CAGCCGGCAA AAAGCGGGGC AGCTGGTGGT CCAGCCCTGG GTGGAGAAAG 1920
TGGATTCCAT CGGGAAACAG CCAGTTGAAG TTTTCTTTAC TAACTGAGAG CAAATGCACC 1980
GAGGCATTTA AAAATAAGCA TATGTTCATA CTGGAATATT TCAAATGAAC AGAAACAACA 2040
CCTAAGGCCC AGATCGATAA ATATTAACTT TGTGACACAT TTACTTCACA ACTTTTTCTA 2100
AACAATTTGG TATACATTAA AACCTACCCC TTCTTCCCCT GGCTCCACTC CCCACTCCCA 2160
TCCTGAAGTT 2170
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